16153-59-6 Usage
Description
(diethoxyphosphoryl)(phenyl)methyl acetate, with the molecular formula C12H17O5P, is a chemical compound that belongs to the ester class, specifically a derivative of phosphoric acid. (diethoxyphosphoryl)(phenyl)methyl acetate is characterized by the presence of two diethoxyphosphoryl groups, one phenyl group, one methyl group, and one acetate group. Its structural complexity and functional groups endow it with a range of applications across different industries.
Uses
Used in Organic Synthesis:
(diethoxyphosphoryl)(phenyl)methyl acetate is used as a reagent for the protection of hydroxyl groups in organic compounds. Its ability to shield these functional groups is crucial in multi-step organic synthesis processes, where the integrity of certain groups must be preserved until a later stage of the reaction sequence.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, (diethoxyphosphoryl)(phenyl)methyl acetate serves as a chemical intermediate. Its role in the synthesis of various pharmaceutical compounds is significant, as it can be transformed into a range of other phosphorus-containing compounds with potential therapeutic applications.
Used in Agrochemical Industry:
(diethoxyphosphoryl)(phenyl)methyl acetate also finds application in the agrochemical industry, where it is utilized as a precursor for the development of new insecticides. Its unique structure and reactivity make it a valuable component in the design and synthesis of novel insecticidal agents.
Used in Chemical Research:
(diethoxyphosphoryl)(phenyl)methyl acetate is also employed in chemical research, where it can be used to study the reactions and properties of phosphorus-containing compounds. This contributes to the broader understanding of phosphorus chemistry and its implications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 16153-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,5 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16153-59:
(7*1)+(6*6)+(5*1)+(4*5)+(3*3)+(2*5)+(1*9)=96
96 % 10 = 6
So 16153-59-6 is a valid CAS Registry Number.
16153-59-6Relevant articles and documents
A new, efficient, and simple method for the one-pot synthesis of α-acetoxyphosphonates from aldehydes under solvent-free conditions
Kaboudin, Babak,Karimi, Masoumeh
, p. 5324 - 5327 (2006)
A simple, efficient, and new method has been developed for the synthesis of α-acetoxyphosphonates from aldehydes through a one-pot reaction of aldehydes with diethylphosphite in the presence of acetic anhydride under solvent-free conditions using magnesiu
Iron-doped single-walled carbon nanotubes as new heterogeneous and highly efficient catalyst for acylation of alcohols, phenols, carboxylic acids and amines under solvent-free conditions
Sharghi, Hashem,Jokar, Mahboubeh,Doroodmand, Mohammad Mahdi
experimental part, p. 426 - 442 (2011/04/15)
Iron-doped single-walled carbon nanotubes (Fe/SWCNTs) represent an efficient and new heterogeneous reusable catalyst for the acylation of a variety of alcohols, phenols, carboxylic acids and amines with acid chlorides or acid anhydrides under solvent-free conditions. The reactions of various primary, secondary, tertiary, and benzylic alcohols, diols, phenols, as well as aromatic and aliphatic amines give acylated adducts in good to excellent yields.
Facile and high-yielding preparation of α-acetoxyphosphonates from α-hydroxyphosphonates assisted by microwave irradiation
Firouzabadi, Habib,Iranpoor, Nasser,Sobhani, Sara,Amoozgar, Zohreh
, p. 1771 - 1774 (2007/10/03)
A convenient and eco-friendly procedure is described for the efficient preparation of a variety of α-acetyloxyphosphonates from their corresponding α-hydroxyphosphonates using acetic anhydride under microwave irradiation in the absence of solvent.
